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Edinburgh Research Explorer Proteins that associate with lamins: many faces, many functions Citation for published version: Schirmer, EC & Foisner, R 2007, 'Proteins that associate with lamins: many faces, many functions', Experimental Cell Research, vol. 313, no. 10, pp. 2167-79. https://doi.org/10.1016/j.yexcr.2007.03.012 Digital Object Identifier (DOI): 10.1016/j.yexcr.2007.03.012 Link: Link to publication record in Edinburgh Research Explorer Document Version: Peer reviewed version Published In: Experimental Cell Research General rights Copyright for the publications made accessible via the Edinburgh Research Explorer is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The University of Edinburgh has made every reasonable effort to ensure that Edinburgh Research Explorer content complies with UK legislation. If you believe that the public display of this file breaches copyright please contact [email protected] providing details, and we will remove access to the work immediately and investigate your claim. Download date: 10. Oct. 2021 Proteins That Associate With Lamins: Many Faces, Many Functions Eric C. Schirmer 1 and Roland Foisner 2 1The Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3JR, United Kingdom, and 2Max F. Perutz Laboratories, Department of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria Email addresses for correspondence: [email protected] [email protected] Keywords: chromatin, lamin, nuclear envelope, nuclear structure Author for internal correspondence: Roland Foisner Max F. Perutz LaboratoriesMedical University of Vienna, Dr. Bohr-Gasse 9/3, A-1030 Vienna, Austria. Email: [email protected]: +43-1-4277-61680, FAX: +43-1-4277-9616 Abstract Lamin-associated polypeptides (LAPs) comprise inner nuclear membrane proteins tightly associated with the peripheral lamin scaffold as well as proteins forming stable complexes with lamins in the nucleoplasm. The involvement of LAPs in a wide range of human diseases may be linked to an equally bewildering range of their functions, including sterol reduction, histone modification, transcriptional repression, and Smad- and β-catenin signaling. Many LAPs are likely to be at the center of large multi- protein complexes, components of which may dictate their functions, and a few LAPs have defined enzymatic activities. Here we discuss the definition of LAPs, review their many binding partners, elaborate their functions in nuclear architecture, chromatin organization, gene expression and signaling, and describe what is currently known about their links to human disease. Introduction The eukaryotic nucleus is a complex organelle with essential functions in genome stability, DNA replication and gene expression. It is structurally and functionally organized into distinct sub-compartments, most prominently the nuclear envelope (NE), which separates nuclear and cytoplasmic activities. The NE is comprised of three major structures (Fig. 1) [1,2]: i) two concentric membrane layers, the outer (ONM) and the inner (INM) nuclear membrane facing the cytoplasm and nucleoplasm, respectively, and separated by the perinuclear lumen; ii) nuclear pore complexes (NPCs) inserted into the double membrane, which mediate nucleo- cytoplasmic exchange of components, and iii) the nuclear lamina protein meshwork that is tightly associated with the INM and provides mechanical stability. The ONM is directly linked to and functionally related to the endoplasmic reticulum (ER) and thus contains ribosomes and other ER proteins. Yet a subset of ONM proteins is unique and not shared with the ER. The INM (although joined with the ONM at NPCs) contains its own unique group of integral membrane proteins that selectively and efficiently target to the INM [3,4]. Many of these INM proteins are components of the nuclear lamina, the core of which is formed by the nuclear-specific, type V intermediate filament lamin proteins. Details of lamins are covered elsewhere in this issue; however, critical to this review is that there are different lamin subtypes: B-type lamins expressed throughout development, and A-type lamins found predominantly in differentiated cells [5,6]. Lamins are post-translationally modified by farnesylation [7]. B-type lamins are permanently farnesylated and thus tightly associated with the INM, in contrast with A-type lamins that either are not farnesylated at all or have the farnesyl group removed by an additional post-translational proteolytic cleavage of the C-terminal 15 residues. The transient farnesylation of lamin A may facilitate its incorporation into the lamina, but after cleavage it should be less tightly associated with the membrane and accordingly, a subfraction of lamin A (estimated at ~5 to 10%) can also be found in the nuclear interior [8]. Multiple stable interactions of lamins with INM proteins within the nuclear lamina are fundamental for the mechanical integrity of the NE. This review focuses on mammalian lamin-associated proteins, most of which are components of the NE and the lamina. We attempt to resolve confusion between the terms lamin-versus lamina-associated polypeptides, which have been synonymously used in literature, and describe interactions, dynamics and potential functions of the best studied lamin-associated polypeptides in mammals, as well as their potential involvement in human diseases. Definition of LAPs as lamin-associated polypeptides The term LAP was originally used to designate “lamina-associated polypeptides”, INM proteins stably associated with the lamina at the nuclear periphery. These proteins bound lamins and cofractionated with lamins upon extraction with buffers containing high concentrations of monovalent salts and non-ionic detergents [9,10]. As the lamina is restricted to the nuclear periphery, LAPs by this definition are located at the NE. However, thereafter the term LAP has also been used for lamin- associated polypeptides, including proteins associated with the ~5% of lamins not located at the nuclear periphery. As the intranuclear lamins are presumably not assembled into a filamentous structure like in the lamina, epitopes may be accessible in nucleoplasmic lamins that are masked in filaments and thus enable interactions with a different set of binding partners. In both cases, however, the term “associated” is meant to indicate a stable or protracted interaction with lamins or lamin complexes biochemically defined by resistance to extraction with salt and detergent. In contrast proteins that interact with lamins transiently upon activation of specific signaling pathways or during the cell cycle or differentiation would be referred to as lamin- interacting polypeptides. In this review we use the more general definition of LAPs defining proteins stably associated with peripheral and internal lamin complexes. One aspect of this biochemical definition of LAPs is that the interaction with lamins can also be indirect. A LAP could bind another LAP that binds to lamins and still resist the harsh extraction conditions. Clearly defined LAPs LAP1 and LAP2 (now known as LAP2 β) were identified by monoclonal antibodies generated against lamina-enriched fractions of rat liver nuclei [9,10]. Both proteins were determined to be integral membrane proteins by biochemical means and to reside at the NE and INM by immunofluorescence and immunogold electron microscopy. Moreover, they bound lamins in vitro . Thus LAPs 1 and 2 have all the characteristics of the most stringent definition of a LAP, although they showed quite different extractabilities at different salt concentrations [9]. The antibody to LAP1 recognized three proteins designated LAP1A, B and C, and cloning of LAP1C [11] indicated that these forms are derived by alternative splicing and expressed in a developmentally regulated manner. Co-precipitation confirmed binding of LAP1C to lamin B [12], but the other LAP1 variants have not been analyzed further. Analysis of the human genomic sequence indicates that the LAP1 gene may have a plenitude of splice variants but this has not been followed up yet. Much more has been revealed on the LAP2 proteins since their initial identification. Cloning of the rat, mouse and human cDNAs and genes [13,14,15,16] identified 6 alternatively spliced isoforms LAP2 α, β, γ, δ, ε, and ζ, all of which, except for LAP2 α and ζ, contain a single C-terminal transmembrane domain and a long nucleoplasmic N-terminus [17]. The first described LAP2 antibodies recognized only LAP2 β, the largest transmembrane LAP2 that binds preferentially lamin B [9,18]. The smaller isoforms, which lack specific regions in the nucleoplasmic domain, have yet to be tested for their lamin binding activity. LAP2 α is unique, as it shares only the N-terminal third with the other isoforms and contains a distinct large C-terminus without a transmembrane domain. Accordingly LAP2 α localizes to the nuclear interior [19], where it forms stable complexes with A-type lamins [20]. Although LAP2 α is resistant to detergent/salt extraction [19] and binds lamins it clearly is not a lamina-associated protein as it is not part of the peripheral lamina. It represents an example of a lamin-associated protein that forms stable and protracted complexes with lamins outside the lamina. Database searches have revealed a 40 amino acid-long motif

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